CN107002026A - Culture media composition for preparing botulin toxin - Google Patents
Culture media composition for preparing botulin toxin Download PDFInfo
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- CN107002026A CN107002026A CN201680004194.XA CN201680004194A CN107002026A CN 107002026 A CN107002026 A CN 107002026A CN 201680004194 A CN201680004194 A CN 201680004194A CN 107002026 A CN107002026 A CN 107002026A
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
- C12N1/20—Bacteria; Culture media therefor
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/14—Hydrolases (3)
- C12N9/48—Hydrolases (3) acting on peptide bonds (3.4)
- C12N9/50—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
- C12N9/52—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from bacteria or Archaea
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
- C07K14/33—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Clostridium (G)
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N5/00—Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P21/00—Preparation of peptides or proteins
- C12P21/02—Preparation of peptides or proteins having a known sequence of two or more amino acids, e.g. glutathione
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y304/00—Hydrolases acting on peptide bonds, i.e. peptidases (3.4)
- C12Y304/24—Metalloendopeptidases (3.4.24)
- C12Y304/24069—Bontoxilysin (3.4.24.69), i.e. botulinum neurotoxin
Abstract
The present invention relates to the culture media composition for producing botulin toxin, and more particularly, to the culture media composition for cultivating the fusobacterium kind that can produce botulin toxin.Peptone of the culture media composition of the present invention comprising pig peptone and at least one plant origin being selected from the group：Pea hydrolysate, cottonseed hydrolysis thing and wheat gluten hydrolysate.Using the peptone containing plant origin, pig peptone and mineral matter according to the medium culture clostridium botulinum of the present invention when, the growth rate of the bacterium in culture medium than the culture medium of the culture medium that uses at present and the peptone for only including plant origin it is every kind of in rate of bacterial growth it is high.In addition, when the culture medium using the present invention, the botulin toxin of high concentration can be produced by cultivating bacterium in a secured manner.
Description
Invention field
The present invention relates to the culture media composition for producing botulin toxin, and more particularly, to for cultivating
The culture media composition of the bacterial strain of the fusobacterium (Clostridium) of botulin toxin can be produced.The culture medium of the present invention
Peptone of the composition comprising pig peptone and at least one plant origin being selected from the group：Pea (garden pea) is hydrolyzed
Thing, cottonseed hydrolysis thing and wheat gluten (wheat gluten) hydrolysate.
Background of invention
Since the nineties in 19th century, it has been found that a variety of fusobacteriums of secretory nerve uremic toxins
(Clostridium) bacterial strain, and sign (Schant, E.J. from the toxin of these bacterial secretories have been carried out within 70 years in the past
Deng Microbiol.Rev., 56:80,1992).
From neurotoxin derived from clostridium species, i.e. botulin toxin, according to its serological property, it is divided into seven species
Type (A to G types).Every kind of toxin has size about 150kDa toxin protein, and naturally includes several nothings in connection
The compound of toxic protein.Medium compound (300kDa) is made up of toxin protein and non-toxic nonhemagglutinin albumen, and
Large complex (450kDa) and very big compound (900kDa) are made up of the medium sized compound combined with hemagglutinin
(Sugiyama,H.,Microbiol.Rev.,44:419,1980).Known such non-toxic hemagglutinin function is protection poison
Element is from the low pH in intestines and various albumen enzyme effects.
Toxin, to be synthesized with molecular weight about 150kDa single polypeptide, then passes through the work of intracellular protein enzyme in cell
With or manually enzyme such as trypsin treatment cuts into two units at 1/3 position N-terminal end：Light chain (L；Point
Son amount：50kDa) with heavy chain (H；Molecular weight：100kDa).Compared with single polypeptide, the toxin of cutting has the poison greatly increased
Property.Two units are connected to each other by disulfide bond and have a different functions.Acceptor (the Park.M.K. of heavy chain combination target cell
Deng FEMS Microbiol.Lett., 72:243,1990), and function be low pH (pH 4) and biological membrane interaction with
Form passage (Mantecucco, C. etc., TIBS., 18:, and light chain can be oozed by using detergent when it 324,1993)
Saturating cell or when importing cell by electroporation etc. with interference neurotransmitter secretion pharmacological activity (Poulain, B. etc.,
Proc.Natl.Acad.Sci.USA.,85:4090,1988)。
Toxin suppresses the acetylcholine exocytosis at the cholinergic pre-synapse of neuromuscular junction to cause weakness.It has been thought that
Toxicity even is shown with the processing of very small amount of toxin, this has pointed out toxin to have any enzymatic activity (Simpson, L.L.
Deng Ann.Rev.Pharmacol.Toxicol., 26:427,1986).
According to nearest report, toxin has metallopeptidase activity, and its substrate includes synaptobrevin
(synaptobrevin), syntaxin (syntaxin), 25kDa synaptosomal related proteins (SNAP25) etc., they are
The unit protein of exocytosis multi mechanism compound thing.Each type of toxin uses one of above-mentioned three kinds of protein to be used as its substrate, and
And known B, D, F and G type toxin cuts synaptobrevin at specific site, A and E type toxin is cut at specific site
SNAP25, and c-type cuts syntaxin (Binz, T. etc., J.Biol.Chem., 265 at specific site:9153,
1994)。
Specifically, it is known that Botox is dissolved in pH 4.0-6.8 dilute aqueous solution.Known stabilization it is nontoxic
Property protein is separated in about more than 7 pH with neurotoxin, and therefore toxicity is gradually lost.Specifically, it is known that toxicity with
PH and temperature are raised and reduced.
Even if botulin toxin is also on a small quantity fatal to human body, and easily a large amount of productions.Therefore, it is with anthrax bud
Spore bacillus (Bacillus anthracis), yersinia pestis (Yersinia pestis) and variola virus (smallpox
Virus four mcroorganism terrorist weapons) are constituted together.However it has been found that when Botox is with not systematically influence human body
When dosage is injected, it can make the local Muscle paralysis in injection site.Based on this feature, Botox can use
In the application of wide scope, including smoothing wrinkle agent (winkle removing agent), treatment spastic hemiplegia and cerebral palsy
Medicament etc..Therefore, the demand to Botox has increased, and has actively developed on production clostridium botulinum poison
The research of the method for element is to meet demand.
At present typical commercial product be can be from Allergan, Inc., commercially available from USA(A type clostridium botulinums
The purified neurotoxin complex of toxin).100 unitsBottle by about 5ng Botox it is pure
Change neurotoxin complex, 0.5mg human serum albumins and 0.9mg sodium chloride composition, and use the Sterile Saline of preservative free
(0.9% sodium chloride injection) is rebuild.Other commercial products include being purchased from Ipsen Ltd., UK's(meat poisoning shuttle
The compound of bacterium A types toxin and hemagglutinin, it has lactose and human serum in the pharmaceutical composition containing botulin toxin
Albumin, and rebuild using preceding using 0.9% sodium chloride), Solstice Neurosciences are purchased from, Inc's(comprising Type B Toxins Toxins, human serum albumins, sodium succinate and sodium chloride Injectable solution (about 5.6
pH))。
Contain animal component for cultivating the culture medium of clostridium botulinum, the culture medium is generally employed to produce clostridium botulinum poison
The method of element, as disclosed in Korean Patent No.10-1339349.Therefore, if being referred to as the work for causing TSE
It is comprised in the animal anomaly prion of agent due to pollution in animal component, then it is for producing botulin toxin
During throw into question.
TSE (TSE) is referred to as causing the neurodegenerative disease of neuron serious degenerative, and in fact
Example includes BSE (BSE), scrapie (Scrapie), Creutz Fei Erte-Jacob (Creutzfeldt-
Jakob) sick (CJD), Jie Ciman-Si Tuosile-Shi Yinke (Gerstmann-Straussler-Scheinker) syndrome, storehouse
Shandong disease (Kuru), infectious mink encephalopathy (transmissible mink encephalopathy), chronic wasting disease
(chronic wasting disease), cat spongiform encephalopathy (feline spongiform encephalopathy) etc., its
Influence humans and animals.BSE is reported by species barrier, or even infects the mankind.
Cause the agent of TSE (TSE) to have the feature that it does not have immunogenicity, and dive
The volt phase (incubation period) is long.It is can be seen that from the histopathological analysis of the BSE cow brain tissues influenceed due to right
Special spongy vacuole is formd in the damage of neuron and the deposition of unusual protein fibres, brain.
The reason for TSE is the proteinacious infectious particles of referred to as abnormal prion.With needing the general virus of nucleic acid not
Together, the infectious particles that abnormal prion is made up of the independent protein without nucleic acid.On TSE, it is known that when being used as infection
Property particle abnormal prion (PrPsc) and normal Prion (PrPc) when combining, be translated into pathogenic prion, then
(Prusiner SB, Alzheimer Dis Assoc Disord., 3 are accumulated in brain:52-78,1989).
Creutzfeldt-Jakob disease is a kind of nerve change of one among a thousand's class TSE (TSE)
Property disease, wherein infectious agent is clearly the abnormal hypotype (isoform) of prion protein.In six months, with Crow she
The individual of Ci Feierte-cortico-striatal spinal degeneration can deteriorate into akinetic mutismus (akinetic from the complete health status in surface
mutism).Therefore, the medicine from the biological agent such as botulin toxin obtained containing the product using animal origin may be present
The potential risk of the disease (such as gram refined Cotard) of prion mediation is obtained in the administration of composition.Therefore, if medicine group
Prepared by the drug substance that compound is produced by the composition using animal origin, then it can make patient by the various pathogen of receiving or biography
Contaminate former potential risk.
Under this technical background, it has been found by the present inventors that coming when the plant without TSE (TSE) will be included
The culture medium of the peptone in source, mineral matter and the pig peptone (the pig peptone of such as TSE certifications) without TSE is used for clostridium botulinum
Risk of the culture to prevent the disease of above-mentioned prion mediation when, can exclude generation can be in the culture medium used at present
The risk for the disease that prion present in (initial medium) mediates, and growth rate of the clostridium botulinum in the culture medium
Compared with the culture medium and the growth rate of the clostridium botulinum only in the culture medium of the peptone comprising plant origin that use at present
It can be increased, thus complete the present invention.
Summary of the invention
Technical problem
It is an object of the invention to provide culture media composition, it infects wind comprising no TSE (TSE)
The peptone of the plant origin of danger and the pig peptone without TSE infection risks, and the method for producing botulin toxin, its
Improve the production of botulin toxin by cultivating clostridium botulinum in culture media composition.
Technical scheme
To achieve these goals, the invention provides the culture media composition for cultivating clostridium botulinum, the culture
Based composition and use thereof in packaging is included：The peptone of at least one plant origin being selected from the group：Pea hydrolysate, cottonseed hydrolysis thing and wheat flour
Muscle hydrolysate；With pig peptone.
The present invention also provides the method for producing botulin toxin, comprises the following steps：(a) culture medium is used
Composition culture clostridium botulinum is to produce botulin toxin；And the botulin toxin of remanufacture (b).
Brief description
Fig. 1 shows the growth of clostridium botulinum in the culture medium (APF culture mediums) of the peptone comprising plant origin.
Fig. 2 shows the meat poisoning shuttle in the culture medium of the peptone comprising plant origin, mineral matter, amino acid and vitamin
The growth of bacterium.
It is after the medium sterilization of peptone, mineral matter, amino acid and vitamin that Fig. 3 display inspections include plant origin
The no result for forming sediment.
Whether Fig. 4 displays form sediment after checking the medium sterilization of the peptone containing plant origin and mineral matter
As a result.
Fig. 5 show by the culture medium (its peptone and mineral matter for containing plant origin) for cultivating bacterium in addition
Add vitamin, amino acid and " the BD Recharge of no glucose and GluTM" obtain culture medium in meat poisoning shuttle
The growth of bacterium.
Fig. 6 show for cultivate bacterium culture medium (it contains the peptone of the plant origin of various species) in meat poisoning
The growth of clostridium.
Fig. 7 shows the FFD isograms and response optimization screened for mineral matter.The isogram of Fig. 7 a high settings；
The isogram set in the middle of Fig. 7 b；The isogram of Fig. 7 c low settings；With Fig. 7 d maximums OD response optimization.
Fig. 8 shows the FFD isograms and response optimization screened for mineral matter.The isogram of Fig. 8 a high settings；
The isogram set in the middle of Fig. 8 b；The isogram of Fig. 8 c low settings；With Fig. 8 d maximums OD response optimization.
Fig. 9 shows the isogram and response optimization screened for phytone.The isopleth set in the middle of Fig. 9 a
Figure；The isogram of Fig. 9 b low settings；With Fig. 9 c maximums OD response optimization.
Figure 10 shows the growth curve of clostridium botulinum in the APF culture mediums of final choice, and toxin concentration change.
Figure 11 a show response surface figure and response optimization, and Figure 11 b are used to screen pig peptone Primatone
P37 or bacterium are usedPeptone No.3.
Figure 12 has graphically illustrated the culture medium (APF of the culture medium used more at present, the peptone comprising plant origin
Culture medium) Clostridium botulinum growth between peptone and the final culture medium (APF+ pigs) of pig peptone comprising plant origin
Time dependence OD values.
The best mode carried out an invention
In the present invention, the culture medium that the culture media composition of animal protein free (APF) shows and used at present is (initial
Culture medium) increased Clostridium botulinum growth speed is compared, but do not consider to add the training of the further growth rate of increase bacterium
Base component is supported, and without the risk of the infection such as TSE.Therefore, not yet report is caused into pig peptone (such as TSE that TSE infects
The pig peptone of certification) it is added to APF culture mediums, and check the growth of bacterium in APF culture mediums.Therefore, with present using
Culture medium is compared with the culture medium for the peptone for only including plant origin, and above-mentioned culture medium shows bacteria growth increase.Knot
Really, if using APF culture mediums, can be highly concentrated to produce by cultivating bacterium in a secured manner under conditions of without TSE
The botulin toxin of degree.
TSE influence people and various animals, including goat, sheep, ermine and deer are reported, but not yet reports the TSE in pig
Break out (Jahns H etc., Vet Rec., 159 (5):137-142,2006；Kofler M etc., Schwweiz Arch
Tierheild,148(7):341-342,344-348,2006).Therefore, in the present invention, pig peptone is added to is used to train
The culture media composition of clostridium botulinum is supported, culture media composition is thus prepared, the culture media composition and the culture used at present
Base compared with the culture medium for the peptone for only including plant origin for producing biological agent, such as botulin toxin without causing
The risk of the disease such as Creutzfeldt-Jakob disease (Creutzfeldt-Jacob disease) of PrPC mediation
Increased rate of bacterial growth is shown in method.
As used herein, term " culture medium or initial medium that use at present " mean comprising casein hydrolysate,
The culture medium of yeast extract and thioglycolic acid salt culture medium (it is the medium component of animal origin)." APF is cultivated term
Base (animal protein free media) " means the protein without animal origin, and the peptone containing plant origin, mineral
The culture medium of matter and glucose.
In the example of the present invention, in order to by cultivating meat poisoning shuttle under conditions of without TSE (TSE)
Bacterium produces botulin toxin, prepares the APF culture mediums of the peptone comprising the plant origin without TSE, and with making at present
Culture medium (containing animal component) compares.Results, it can be seen that the optimal medium composition for cultivating clostridium botulinum
It is the peptone comprising plant origin, at least one is selected from KH2PO4、K2HPO4And Na2HPO4Mineral matter, and carbon source (such as Portugal
Grape sugar) culture medium, and it was found that the optimum growh of bacterium in the culture medium.As a result, as shown in table 13, it is determined that for training
The optimum content of the peptone of plant origin in the culture media composition for the final choice for supporting clostridium botulinum is 5g/L Hy-
PeaTM7404、10g/L UltraPepTMCotton and 5g/L HyPepTM4601N, and culture media composition mineral is optimal
Content is 5.5g/L K2HPO4With 3g/L Na2HPO4。
In another example of the present invention, the final choice of peptone of the measurement containing plant origin and mineral matter
The growth pattern and toxin concentration of clostridium botulinum in APF culture mediums.As a result, as shown in table 12 and Figure 10, clostridium botulinum
OD values start increase after culture in 12 hours, and when cultivating 24 hours, culture medium shows 3.5465 OD540nmWith 3.0695
OD600nm.Then, OD values are gradually reduced, and at 48 hours of culture, culture medium showed 0.792 OD540nmWith 0.7224
OD600nm.Toxin concentration in clostridium botulinum culture supernatant starts increase after cultivating 5 hours, and shows 31.41 μ
G/ml end value.When rupturing measurement toxin concentration after bacterium, culture starts to produce toxin, and toxin concentration after 5 hours
Continue to increase, culture is maintained at consistent level after 28 hours, and shows 38.39 μ g/ml end value.
In another example of the present invention, in the culture medium for checking the peptone comprising plant origin and pig peptone
Clostridium botulinum growth.As a result, as shown in table 14, when cultivating bacterium in further including the culture medium of pig peptone, training
Support the high OD values of the culture medium of peptone of the base display than only including plant origin.Especially, display highest bacterial growth speed
The culture medium of rate is used comprising 10g/L Primatone P37 and 10g/L bacteriumPeptone No.3 culture medium, it shows
OD540nmValue 4.951.
In another example of the present invention, in the culture medium for checking the peptone comprising plant origin and pig peptone
The growth pattern of clostridium botulinum.As a result, as shown in table 15, when cultivating 20 hours of bacterial strain, the albumen comprising plant origin
Bacterial growth in the culture medium of peptone and pig peptone is active, and culture medium is shown as the pact of the OD values of commercial medium
About 2.2 times of high OD values that are 11 times high and being the only OD values of the culture medium of the peptone comprising plant origin.In culture bacterium
At 29 hours, the peak OD values of the culture medium of the peptone comprising plant origin and pig peptone are the culture medium that uses at present and only
Every kind of peak OD values of the culture medium of peptone comprising plant origin it is at least 2 times high.Therefore, it can be seen that coming comprising plant
Rate of bacterial growth in the peptone in source and the culture medium of pig peptone in three class culture mediums in those of be highest.
As a result, as shown in table 16, it is determined that (it contains the culture media composition for cultivating clostridium botulinum of final choice
Whether there is the pig peptone of TSE (TSE)) in the optimum content of peptone of plant origin be 5g/L Hy-
PeaTM7404、10g/L UltraPepTMCotton and 5g/L HyPepTMOptimal mineral matter in 4601N, and culture media composition
Content is 5.5g/L K2HPO4With 3g/L Na2HPO4, the content of glucose is 10g/L, and the content of pig peptone is 13g/
L Primatone P37 and 13g/L bacterium are usedPeptone No.3.
Therefore, on the one hand, the present invention relates to the culture media composition for cultivating clostridium botulinum, the culture media composition
Comprising：The peptone of at least one plant origin being selected from the group：Pea hydrolysate, cottonseed hydrolysis thing and wheat gluten hydrolysis
Thing；With pig peptone.
As used herein, term " peptone of plant origin " means the peptone extracted from pea, cottonseed or gluten.
Preferably, the peptone of plant origin can be commercially available Hy-PeaTM7404、UltraPepTMCotton, HyPepTM7504 or
HyPepTM4601N, but not limited to this.Term " pig peptone " means the component extracted from porcine tissue.Preferably, pig peptone can
To be the pig peptone for including the about 54.91-60.69wt% peptides with below 500Da molecular weight, or about 38.48- is included
42.53wt% has the pig peptone of the peptide of below 500Da molecular weight.It is highly preferred that casein hydrolysate can be commercialization
Primatone P37 or bacterium are usedPeptone No.3, but not limited to this.
As used herein, term " peptone of plant origin " or " hydrolysate of plant origin " mean by degrade from
The protein of plant separation and the product that obtains.For example, pea protein peptone (pea hydrolysate) means by degrading from pea
The total protein of separation and the product obtained.In addition, term " pig peptone " or " pig hydrolysate " mean by pig protein of degrading
The product of acquisition.
The degraded of the protein or porcine tissue protein of plant origin is preferably carried out by partial digested.The drop of protein
Solution is preferably carried out by acid treatment, alkali process, ferment treatment, HIGH PRESSURE TREATMENT, heat treatment or physical treatment.It is highly preferred that pig albumen
Peptone can be obtained by ferment treatment.Physical treatment is for example to grind.
Peptone or pig peptone for the plant origin of the present invention are the Partial digestion products of protein, are not only to wrap
Containing the amino acid as single molecule, but also comprising by several peptides constituted to dozens of amino acid, and complete protein point
The mixture of son.
In the present invention, the content of the peptone of plant origin can be 0.1-10w/v% (1- in culture media composition
100g/L), preferably 0.2-5w/v% (2-50g/L), more preferably 0.5-2w/v% (5-20g/L).
In the present invention, culture media composition includes all pea hydrolysates, cottonseed hydrolysis thing and wheat gluten hydrolysate,
And the content ratio of pea hydrolysate, cottonseed hydrolysis thing and wheat gluten hydrolysate can be by weight 1 in culture media composition:
0.24-43.62:0.01-50.57, preferably by weight 1:0.68-14.46:0.09-9.87, more preferably by weight 1:1.6-
2.4:0.6-1.4。
In the present invention, the content of the pig peptone in culture media composition can be 0.2-10w/v% (2-100g/L), excellent
Select 0.4-5w/v% (4-50g/L), more preferably 1-2w/v% (10-20g/L).
In the present invention, pig peptone can be the peptide of the molecular weight comprising about 54.91-60.69wt% with below 500Da
Hydrolysate and/or have comprising about 38.48-42.53wt% below 500Da molecular weight peptide hydrolysate.
In the present invention, if pig protein contains comprising the about 54.91-60.69wt% molecular weight with below 500Da
The hydrolysate of peptide and there is both below 500Da hydrolysates of peptide of molecular weight comprising about 38.48-42.53wt%, then can make
The content (by weight) of the pig peptone is calculated with equation 1 below, and is had comprising about 54.91-60.69wt%
The hydrolysate of the peptide of below 500Da molecular weight and have comprising about 38.48-42.53wt% below 500Da molecular weight peptide
Hydrolysate content ratio can by weight be preferably 1:0.8-1.2.
Equation 1
B >=-0.625*A+12.5, B≤- 1.019*A+53
Wherein
A：There is the content (0- of the hydrolysate of the peptide of below 500Da molecular weight comprising about 54.91-60.69wt%
5.2w/v% (0-52g/L))；
B：There is the content (0- of the hydrolysate of the peptide of below 500Da molecular weight comprising about 38.48-42.53wt%
5.3w/v% (0-53g/L)).
In the present invention, it can also be selected from for cultivating the culture media composition of clostridium botulinum containing carbon source and at least one
K2HPO4(dipotassium hydrogen phosphate), Na2HPO4(sodium dihydrogen phosphate) and KH2PO4The mineral matter of (potassium dihydrogen phosphate).
Herein, the example of carbon source includes but is not limited to monose (such as glucose, fructose etc.), disaccharides (such as malt
Sugar, sucrose etc.), oligosaccharides, polysaccharide (such as dextrin, cyclodextrin, starch), sugar alcohol is (for example, xylitol, D-sorbite, erythrose
Alcohol etc.).
In the present invention, the content of culture media composition mineral can be 0.05-3.5w/v% (0.5-35g/L), excellent
Select 0.1-1.75w/v% (1-17.5g/L), and more preferably 0.25-0.7w/v% (2.5-7g/L).
On the other hand, the present invention relates to the method for producing botulin toxin, comprise the following steps：(a) using upper
Culture media composition culture clostridium botulinum is stated to produce botulin toxin；And the botulin toxin of remanufacture (b).
In the present invention, culture can be carried out under anaerobic, and botulin toxin can selected from A, B, C, D,
The botulin toxin of E, F, G type.
Embodiment
Hereinafter, with reference to embodiment, the more detailed description present invention.It is obvious for those of ordinary skill in the art
It is, the purpose that these embodiments are merely exemplary, and should not be construed as limiting the scope of the present invention.Therefore, reality of the invention
Matter scope will be limited by appended claims and its equivalent.
Embodiment 1：Clostridium botulinum is cultivated in the protein culture medium of plant origin
1-1：Currently used for the composition of the culture medium of culture
Reagent and nutrient media components for the present invention are purchased from Sigma (USA), Kerry Inc. (USA), BD
Biosciences (USA), Gibco Life Technologies (USA) and Quest (USA).
Using the seed culture and main culture of the culture medium progress clostridium botulinum used at present to produce botulin toxin,
The culture medium, which has, includes 2% casein hydrolysate (20g/L), 1% yeast extract (10g/L), 1% glucose (10g/
L) and 0.5% thioglycolic acid salt culture medium (5g/L) composition.Every liter of 5g thioglycolic acids of culture medium for using at present
Salt culture medium is by the enzymic digestion thing of 2.52g caseins, 0.84g yeast extracts, 0.925g dextroses, 0.085g thioglycolic acids
Sodium, 0.42g NaCl, 0.085g Cys, 0.00014g resazurins (Resazurin) and 0.125g bacteriology agar groups
Into.
1-2：The composition of the APF culture mediums used in culture
By removing casein hydrolysate, yeast from the culture medium (initial medium) currently used for culture clostridium botulinum
Extract and thioglycolic acid salt culture medium prepare negative control medium, and the peptone by the way that Four Plants are originated
Candidate (Hy-PeaTM7404、UltraPepTMCotton, HyPepTM7504 and HyPepTM4601N) it is added to negative control medium
In prepare animal protein free (APF) culture medium (table 1).
Table 1 shown compared with the culture medium used at present, the albumen for including plant origin for cultivating clostridium botulinum
The component of the APF culture mediums of peptone.
Table 1
1-3：The seed culture of clostridium botulinum
By 20 μ l clostridium botulinums (South Korea's disease prevention and control center's registration numbers：4-029-CBB-IS-001) be inoculated into containing
In the culture tube of 10ml aseptic culture mediums, the aseptic culture medium has every kind of composition described in embodiment 1-1 and 1-2, and
Primary seed culture (static gas wave refrigerator) 22-30 hours is carried out under anaerobic at 35 DEG C.When confirming primary seed culture
In bacterial growth when, by 8ml primary seed cultures be inoculated into containing 800ml have same medium constitute sterile culture
In 1 liter of blake bottle of base, and secondary seed culture (static gas wave refrigerator) is carried out at 35 DEG C under anaerobic 8-15 hours.
1-4：The main culture of clostridium botulinum
In order to produce botulin toxin by cultivating clostridium botulinum, the main culture of bacterium is carried out.Specifically, 9.3L is prepared
Culture medium with every kind of composition described in embodiment 1-1 and 1-2, is placed in 10 liters of incubators, then culture medium is gone out
Bacterium.Supply nitrogen carries out at 35 DEG C of temperature and 50rpm mixing speed the growth of bacterium to produce anaerobic condition.
The inoculation line being connected by the inoculation mouth with 10 liters of incubators will be secondary in 1 liter of blake bottle in embodiment 1-3
Inoculum is inoculated into 10 liters of incubators.Clostridium botulinum in 10 liters of incubators of culture under conditions of 35 DEG C and 50rpm,
Monitor and record the condition of culture of setting.When more than when Bacteria Culture 100 is small, main culture is terminated.
Pass through the peptone candidate (Hy-Pea that Four Plants are originatedTM7404、UltraPepTMCotton, HyPepTM7504
And HyPepTMThe growth for clostridium botulinum 4601N) being added in animal protein free (APF) culture medium prepared in negative control
With by removing casein hydrolysate, yeast extract and thio from the culture medium (initial medium) (table 1) used at present
Bacterial growth in negative control medium prepared by glycollate culture medium compares.
Therefore, as shown in table 1 and Fig. 1, clostridium botulinum does not grow in negative control medium, but after inoculated bacteria
Start within 24 hours to grow in the initial medium (culture medium used at present), and start within 30 hours after inoculated bacteria containing
Have plant origin peptone culture medium in grow.
Embodiment 2：Meat is cultivated in the culture medium of the peptone containing plant origin, mineral matter, amino acid and vitamin
Malicious clostridium
Due to the clostridium botulinum in culture medium in embodiment 1 by adding the peptone preparation that Four Plants are originated
The growth of clostridium botulinum in growth fraction initial medium is slow, and its solution has been provided below.
1) in order to which audit function is produces the effect of the thioglycolic hydrochlorate of anaerobic condition, (make at present from initial medium
Culture medium) middle removing thioglycolic hydrochlorate, and analyze rate of bacterial growth in the culture medium without thioglycolic hydrochlorate
Change.
2) because slower growth rate can be due to caused by nitrogen source lacks, by the culture medium for Bacteria Culture
Peptone concentration increases by 2 times.
3) it will be obtained by the culture medium that mineral matter, amino acid and vitamin are added to the peptone containing plant origin
Culture medium in clostridium botulinum growth and United States Patent (USP) No.8,012,716 (Allergan) disclosed in APF culture mediums
The growth fraction of clostridium botulinum in (table 2) compared with.
Table 2 shows the composition of the culture medium for cultivating clostridium botulinum, and it contains the peptone of plant origin, mineral
Matter, amino acid and vitamin.
Table 2
As a result, as shown in table 2 and Fig. 2, when culture is thin in the culture medium without thioglycolic hydrochlorate used at present
During bacterium, the speed of growth of bacterium is slower than containing the speed of growth in thio glycollate culture medium in culture medium, indicates thioglycolic
Hydrochlorate influences the growth rate of bacterium.When the peptone concentration in culture medium is increased by twice, bacterium does not give birth in the medium
It is long.In the case of mineral composition, amino acid and vitamin is added to the culture medium containing peptone, the speed of growth of bacterium
It is similar to the speed of growth of bacterium in the culture medium used at present, but sediment is formed after medium sterilization.In addition, it is seen that
The speed of growth of bacterium is similar to the speed of growth of bacterium in the culture medium used at present in Allergan APF culture mediums.
Embodiment 3：Produced by the culture medium of the sterilize peptone containing plant origin, mineral matter, amino acid and vitamin
Raw sediment
In example 2, it was observed that the albumen containing plant origin in APF culture mediums candidate 2 to 4 shown in table 2
In peptone, mineral matter, the speed of growth of clostridium botulinum in the culture medium of amino acid and vitamin and the culture medium used at present
The speed of growth of clostridium botulinum is similar.However, occurring the formation of sediment after medium sterilization, therefore check its reason (table
3)。
Table 3 is shown to be used and the peptone containing plant origin, mineral matter, the use of amino acid and vitamin in sterilizing
In the component of the culture medium of culture clostridium botulinum.
Table 3
As a result, as shown in table 3 and Fig. 3, only mineral matter is added in the culture medium to the peptone containing plant origin
In the case of, sediment is just formed after medium sterilization, the main cause for indicating sediment formation is mineral matter.This be considered as because
For under elevated temperature and pressure conditions, mineral composition interacts during medium sterilization.
Embodiment 4：Pass through the culture medium formation sediment of the sterilize peptone containing plant origin and mineral matter
In order to identify mineral composition that the sediment as caused by confirming in embodiment 3 by sterilizing involves in being formed,
The various combinations of heterogeneity are added in culture medium, then (table 4) are sterilized.
Table 4 show the culture medium for being used to cultivate clostridium botulinum of the peptone containing plant origin and mineral matter into
Point, and medium sterilization result.
Table 4
As a result, as shown in table 4 and Fig. 4, in the culture medium of the peptone containing plant origin and mineral matter, contain
MgSO4·7H2O and K2HPO4Culture medium and contain MgSO4·7H2O and Na2HPO4Culture medium form precipitation after sterilization
Thing.
Embodiment 5：Do not formed in APF culture mediums under conditions of sediment and cultivate clostridium botulinum
When the embodiment 4 that vitamin and amino acid are additionally added to the peptone containing plant origin and mineral matter
When in APF culture mediums, whether the culture for being tested to determine clostridium botulinum may.In addition, being tested to check bacterium
Culture is in peptone and mineral matter without plant origin and containing vitamin, amino acid and/or " without glucose and L- paddy ammonia
The BD Recharge of acid amidesTM" (catalogue numbering 670002, BD Bioscience) (and be free of glucose and Glu
The medium component based on yeast extract) culture medium in whether may (table 5).
Table 5 shows another by the culture medium for being used to cultivate clostridium botulinum to the peptone containing plant origin and mineral matter
Outer addition vitamin, amino acid and " the BD Recharge without glucose and GluTM" obtain nutrient media components,
And the speed of growth of bacterium in the medium.
Table 5
As a result, as shown in table 5 and Fig. 5, only in peptone and KH containing plant origin2PO4、K2HPO4And Na2HPO4
The combination of two or more mineral matters and the culture medium further containing vitamin and amino acid in the case of, meat poisoning shuttle
Bacterium grows after microbionation in 24 hours.In addition, being free of the peptone and mineral matter of plant origin and containing dimension in culture medium
Raw element, amino acid and " the BD Recharge without glucose and GluTM" in the case of, bacterium is after microbionation
Grown in 48 hours.Peptone in a word, for the most suitable culture media composition including plant origin of cultivating clostridium botulinum,
KH2PO4、K2HPO4、Na2HPO4, amino acid and vitamin.
Embodiment 6：Clostridium botulinum is cultivated in the culture medium of the protein containing different plant origins
Tested to check when the various combination for the peptone for adding plant origin in the APF culture mediums to embodiment 5
When clostridium botulinum culture whether may.
Table 6 shows the composition for being used to cultivate the culture medium of clostridium botulinum of the peptone containing different plant origins, with
And check the result whether bacterium grows in the medium.
Table 6
As a result, it is only a kind of in the peptone that Four Plants source is added to culture medium as shown in table 6 and Fig. 6
Or at two kinds, the culture of clostridium botulinum is possible.
In view of the result of embodiment 5 and 6, it can be seen that the albumen of at least one plant origin should be contained in culture medium
Peptone, and the peptone of plant origin can not use " the BD Recharge without glucose and GluTM" (catalogue
Numbering 670002, BD Bioscience) (medium component based on yeast extract without glucose and Glu)
Substitute.
Embodiment 7：For two kinds of experiment in three kinds of mineral matters containing in Selective agar medium
In embodiment 1 to 7, it is determined that the APF culture media compositions for clostridium botulinum culture include glucose, sodium chloride
(NaCl), peptone, three kinds of mineral matters, amino acid and the vitamin in Four Plants source.In these medium components, remove
The medium component being had no significant effect to bacterial growth, to reduce the number of medium component.Therefore, amino acid and dimension are judged
Growth of the raw element to clostridium botulinum is had no significant effect, and herein under judgement, amino acid and dimension are removed from medium component
Raw element.In addition, in order to select two kinds from three quasi-minerals, using the culture media composition culture bacterium shown in table 7, and surveying
Amount inoculated bacteria after 24 hours and 48 hours OD (540nm and 600nm) values and compare.
Table 7 shows the life of the composition and clostridium botulinum in culture medium of the culture medium of the first stage selection from mineral matter
It is long.
Table 7
As a result, as shown in table 7,24 hours after microbionation, the culture medium used at present shows 0.942 OD
(540nm) value, and contain K2HPO4And Na2HPO4APF culture mediums show APF culture mediums in 4.964 highest OD
(540nm) value.In addition, 48 hours after microbionation, containing KH2PO4And Na2HPO4APF culture mediums show highest OD values
With active bacterial growth.
Meanwhile, as shown in Figure 7, depict the K with high main effect2HPO4And Na2HPO4Isogram.As a result, with
K2HPO4And Na2HPO4Concentration increase, OD values increase.Also, when with KH2PO4=0g/L, K2HPO4=5.5g/L and
Na2HPO4When mineral matter is added to culture medium by=5g/L concentration, clostridium botulinum shows highest growth.
Meanwhile, in order to confirm bacteria cultivation results according to the addition of more accurate mineral matter, the is carried out using response phase method
Two-stage tests.Because culture media composition there can not be negative value, tested using CCF (Central Composite face) planned design, and
Carried out by cultivating bacterium in the culture media composition shown in table 8.Then, by experimental result and the FFD previously carried out
Result combine and carry out statistical analysis.
Table 8 shows clostridium botulinum in the composition and culture medium of the culture medium obtained by the selection of the second stage of mineral matter
Growth.
Table 8
Drawing isoline figure simultaneously is used to compare.As shown in Figure 8, with KH2PO4Concentration is reduced, the increase of OD values.When comparing
It is as a result different from FFD result due to curvature effect during optimum condition, and K2HPO4Value it is identical, but Na2HPO4's
Value becomes from 5g/L turns to 3.1313g/L.Therefore, confirm that the optimal mineral matter condition of culture medium is 5.5g/L by statistical analysis
K2HPO4With 3g/L Na2HPO4。
Embodiment 8：For the experiment of the peptone of plant origin contained in Selective agar medium
As shown in Table 9 and Table 10, the peptone for merging plant origin is designed according to mixture, and checks the plant containing combination
The growth of clostridium botulinum in the culture medium of the peptone in thing source.
Table 9 shows the composition for the culture medium for selecting the peptone of plant origin to be obtained by the first stage and using training
Support the growth of the clostridium botulinum of base.
Table 9
Table 10 shows that the composition of the culture medium obtained by the second stage selection of the peptone of plant origin is closed and used
The growth of the clostridium botulinum of culture medium.
Table 10
As a result, as shown in Figure 9, drawing isoline figure and for comparing.It is determined that corresponding to component C HyPepTM7504 pairs
The growth of clostridium botulinum has minimum influence.Based on this measure, HyPep is excluded from nutrient media componentsTM7504.In a word, it is determined that
The composition of the peptone of the plant origin of the final choice contained in culture medium includes 5g/L Hy-PeaTM7404、10g/L
UltraPepTMCotton and 5g/L HyPepTM4601N。
Embodiment 9：The culture of the clostridium botulinum in culture medium containing NaCl or without NaCl
The culture media composition used in embodiment 1 to 8 contains (0.5g/L) NaCl on a small quantity.For the concentration according to NaCl
Change checks the growth of clostridium botulinum, the content of NaCl in medium is adjusted to 0 to 1g/L scope, then in the medium
Cultivate bacterium.
Table 11 shows clostridium botulinum in the composition and culture medium of the culture medium containing NaCl for cultivating clostridium botulinum
Growth.
Table 11
Therefore, as shown in Figure 11 a and 11b, no matter whether culture medium contains NaCl, the no difference of growth of bacterium.Cause
This, NaCl is excluded from final APF medium components.
Embodiment 10：Measure the growth pattern and toxin concentration of clostridium botulinum in the APF culture mediums of final choice
Clostridium botulinum is inoculated into the clostridium botulinum culture medium for the final choice that the result based on embodiment 1 to 9 is determined
(10g/L glucose, 5g/L Hy-PeaTM7404、10g/L UltraPepTMCotton, 5g/L HyPepTM4601N、5.5g/L
K2HPO4And 3g/L Na2HPO4), then measure the growth pattern and toxin concentration of bacterium.
Table 12 shows the time dependence OD values and toxin of the clostridium botulinum grown in the APF culture mediums of final choice
Concentration.
Table 12
As a result, as shown in table 12 and Figure 10, OD values start increase after culture clostridium botulinum 12 hours, and are cultivating 24
Hour culture medium shows 3.5465 OD540nmWith 3.0695 OD600nm.Then, OD values are gradually reduced, and small in culture 48
When, culture medium shows 0.792 OD540nmWith 0.7224 OD600nm.Toxin concentration in clostridium botulinum supernatant is in culture 24
Start increase after hour, and show the μ g/ml of end value 31.41.When rupturing measurement toxin concentration after bacterium, cultivate 5 hours
After start to produce toxin, and toxin concentration continues to increase, and culture is maintained at consistent level after 28 hours, and shows final
The μ g/ml of value 38.39.
In a word, APF (the no animal eggs for the final choice that the result based on embodiment 1 to 10 is determined are summarized in table 13
The culture medium of white matter) composition.
Table 13
Embodiment 11：The growth of meat poisoning carboxyl in the culture medium of peptone containing plant origin and pig peptone
Although the APF culture media compositions determined via embodiment 1 to 10 show increasing compared with the culture medium used at present
Plus rate of bacterial growth, it is contemplated that addition further improve rate of bacterial growth and do not cause TSE infect etc. wind
The nutrient media components of danger.As a result, the pig peptone that not yet report causes TSE to infect is added to APF culture mediums, and checks institute
Bacterial growth in the culture medium obtained.
The APF cultures that pig peptone of the one or two without TSE is determined added to the result based on embodiment 1 to 10
Base.Specifically, used in the peptone containing plant origin and pig peptone Primatone P37 and/or bacteriumPeptone
By clostridium botulinum culture 24 hours and 48 hours in No.3 culture media composition, and pass through the OD during measuring culture
(540nm, 600nm) value checks the growth (table 14) of bacterium.In addition, measurement result is carried out into statistics credit using statistics program
Analysis, thus selects the culture media composition in the display highest growth in 24 hours of culture bacterium.
Table 14 shows the component of the culture medium for cultivating clostridium botulinum, and the culture medium contains the albumen of plant origin
Peptone, mineral matter and pig peptone.
Table 14
As a result, as shown in table 14, when cultivating bacterium in the culture medium further containing pig peptone, culture medium shows
Show the OD value higher than the OD values of the only culture medium of the peptone containing plant origin.Especially, display highest bacterial growth speed
The culture medium of rate is used containing 10g/L Primatone P37 and 10g/L bacteriumThe culture medium of peptone, it shows OD540nm
Value 4.951.
Meanwhile, in order to determine the condition that can maximize bacterial growth, experiment is extended into response surface method, and will
The result of response surface method carries out statistical analysis using statistics program.In addition, as shown in Figure 11 (A), drawing response
Isogram, and result, find the condition of maximizing bacterial growth in scope of experiment.In addition, calculating maximizing bacterium
The condition of growth.As a result, as shown in Figure 11 (B), used containing 13.131g/L Primatone P37 and 12.727g/L bacteriumPeptone No.3 culture medium shows OD540nmValue 4.8718, it corresponds to highest rate of bacterial growth.Train for convenience
Based composition and use thereof in packaging is supported, every kind of extra component is used with 13g/L amount in subsequent experiment.
Embodiment 12：The growth pattern of meat poisoning carboxyl in the culture medium of peptone containing plant origin and pig peptone
Using the peptone containing plant origin and the culture media composition of pig peptone determined in embodiment 1 to 11,
Clostridium botulinum is cultivated, and checks the growth pattern (being shown in Table 15) of bacterium in culture medium.
Table 15 shows the culture medium used more at present, (APF is cultivated the culture medium of the peptone comprising plant origin
Base) time of Clostridium botulinum growth between peptone and the final culture medium (APF+ pigs) of pig peptone comprising plant origin
Dependence OD values.
Table 15
As a result, as shown in table 15 and Figure 12, in culture 20 hours of bacterial strain, the peptone comprising plant origin and pig egg
Bacterial growth in the culture medium of white peptone is active, and culture medium is shown as about the 11 of the OD values of the culture medium used at present
About 2.2 times of high OD values that are high again and being the only OD values of the culture medium of the peptone comprising plant origin.The 29 of culture bacterium
Hour, the peak OD values of the culture medium of the peptone comprising plant origin and pig peptone are the culture medium used at present and only contained
Every kind of peak OD values of the culture medium of the peptone of plant origin it is at least 2 times high.Therefore, it can be seen that containing plant origin
Rate of bacterial growth in the culture medium of peptone and pig peptone in three kinds of culture mediums in those of be highest.
In a word, shown in the result based on embodiment 11 and 12, table 16 except animal protein free (APF) culture medium
The composition of the outer final choice comprising pig peptone.
Table 16
Industrial applicibility
As described above, working as the culture according to the present invention of the peptone containing plant origin, pig peptone and mineral matter
When base is used for the culture of clostridium botulinum, the speed of growth of bacterium is than the culture medium that uses at present and only containing plant in culture medium
The culture medium of the protein in source it is every kind of in bacterium the speed of growth it is high.In addition, when the culture medium using the present invention, can lead to
Cross and cultivate bacterium in a secured manner to produce the botulin toxin of high concentration.
Although the present invention is described in detail with reference to specific features, it will be apparent to those skilled in the art
, this specification do not limit the scope of the invention only for preferred embodiment.Therefore, essential scope of the invention
It will be limited by appended claims and its equivalent.
Claims (12)
1. one kind is used for the culture media composition for cultivating clostridium botulinum (Clostridium botulinum), the culture medium group
Compound is included：
The peptone of at least one plant origin being selected from the group：Pea hydrolysate, cottonseed hydrolysis thing and wheat gluten hydrolysate；
With
Pig peptone.
2. the culture media composition of claim 1, wherein including the albumen of the plant origin with 0.1-10w/v% content
Peptone.
3. the culture media composition of claim 1, wherein the culture media composition is with by weight 1:0.24-43.62:
0.01-50.57 ratio includes the pea hydrolysate, the cottonseed hydrolysis thing and described small in the culture media composition
Wheat gluten hydrolysate, condition, which is the culture media composition, includes the pea hydrolysate, the cottonseed hydrolysis thing and described small
Wheat gluten hydrolysate.
4. the culture media composition of claim 1, wherein including institute in the culture media composition with 0.2-10w/v% content
State pig peptone.
5. the culture media composition of claim 1, wherein the pig peptone is having comprising about 54.91-60.69wt%
The hydrolysate of the peptide of below 500Da molecular weight, and/or there is below 500Da molecular weight comprising about 38.48-42.53wt%
The hydrolysate of peptide.
6. the culture media composition of claim 5, wherein calculating containing for the pig peptone by weight using equation 1 below
Amount, condition is the hydrolysis that the pig peptone contains the peptide comprising the about 54.91-60.69wt% molecular weight with below 500Da
Thing and there is both below 500Da hydrolysates of peptide of molecular weight comprising about 38.48-42.53wt%：
Equation 1
B≥-0.625*A+12.5,B≤-1.019*A+53
Wherein
A：There is the content (0-5.2w/ of the hydrolysate of the peptide of below 500Da molecular weight comprising about 54.91-60.69wt%
V%)；
B：There is the content of the hydrolysate of the peptide of below 500Da molecular weight comprising about 38.48-42.53wt%.
7. the culture media composition of claim 1, wherein the peptone of the plant origin or the pig peptone are subjected at enzyme
Reason.
8. the culture media composition of claim 1, it further includes carbon source, and at least one mineral matter being selected from the group：
K2HPO4(dipotassium hydrogen phosphate), Na2HPO4(disodium hydrogen phosphate) and KH2PO4(potassium dihydrogen phosphate).
9. the culture media composition of claim 8, wherein being included in the culture media composition with 0.05-3.5w/v% content
The mineral matter.
10. a kind of method for producing botulin toxin, it comprises the following steps：
(a) usage right requires any one of 1 to 9 culture media composition culture clostridium botulinum to produce botulin toxin；
And
(b) botulin toxin of remanufacture.
11. the method for claim 10, wherein carrying out the culture under anaerobic.
12. the method for claim 10, wherein the botulin toxin is selected from the group：BoNT/A, B, C,
D, E, F and G.
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| KR1020150059656A KR101723168B1 (en) | 2015-04-28 | 2015-04-28 | Medium Composition for Preparing Botulinum Toxin |
| KR10-2015-0059656 | 2015-04-28 | ||
| PCT/KR2016/004432 WO2016175567A1 (en) | 2015-04-28 | 2016-04-28 | Medium composition for preparing botulinum toxin |
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| EP (1) | EP3289071A4 (en) |
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| KR101723168B1 (en) * | 2015-04-28 | 2017-04-05 | 주식회사 대웅 | Medium Composition for Preparing Botulinum Toxin |
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| US6558926B1 (en) | 1999-07-16 | 2003-05-06 | Massachusetts Institute Of Technology | Method for production of tetanus toxin using media substantially free of animal products |
| US7148041B2 (en) * | 2003-09-25 | 2006-12-12 | Allergan, Inc. | Animal product free media and processes for obtaining a botulinum toxin |
| US7160699B2 (en) | 2003-09-25 | 2007-01-09 | Allergan, Inc. | Media for clostridium bacterium and processes for obtaining a clostridial toxin |
| RU2255761C1 (en) | 2004-07-01 | 2005-07-10 | Общество с ограниченной ответственностью "Токсины и сопутствующие продукты" | Preparation for treatment of muscular dystonia from toxin of culture clostridium botulinum and method for its preparing |
| WO2006042542A2 (en) * | 2004-10-19 | 2006-04-27 | Statens Serum Institut | Production of tetanus, diphtheria, and pertussis toxins and toxoids using fermentation media containing no components of animal or soy origin |
| AU2005327458B2 (en) * | 2005-03-03 | 2011-12-15 | Allergan, Inc. | Animal product free system and process for purifying a botulinum toxin |
| CA2602440A1 (en) * | 2005-09-16 | 2007-04-05 | Allergan, Inc. | Compositions and methods for the intraocular transport of therapeutic agents |
| KR100680318B1 (en) * | 2005-12-16 | 2007-02-08 | 최성현 | Nutrient broth for culturing of microorganism |
| US7811560B2 (en) * | 2006-01-30 | 2010-10-12 | Auxilium Us Holdings, Llc | Compositions and methods for treating collagen-mediated diseases |
| FR2918671B1 (en) * | 2007-07-10 | 2010-10-15 | Sanofi Pasteur | GROWING MEDIUM OF HAEMOPHILUS INFLUENZAE TYPE B. |
| KR20090120222A (en) | 2008-05-19 | 2009-11-24 | (주)메디톡스 | Method of producing clostridium botulinum toxin using a media containing plant derived components and a flexible closed container |
| KR101339349B1 (en) | 2013-08-02 | 2013-12-09 | 주식회사 대웅 | Methods for preparing botulinum toxin |
| KR101723167B1 (en) * | 2015-04-28 | 2017-04-05 | 주식회사 대웅 | Medium Composition for Preparing Botulinum Toxin |
| KR101729251B1 (en) * | 2015-04-28 | 2017-04-21 | 주식회사 대웅 | Medium Composition for Preparing Botulinum Toxin |
| KR101723168B1 (en) * | 2015-04-28 | 2017-04-05 | 주식회사 대웅 | Medium Composition for Preparing Botulinum Toxin |
| KR101775682B1 (en) * | 2015-11-30 | 2017-09-06 | 주식회사 대웅 | Methods for Preparing Botulinum Toxin |
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- 2016-04-28 EP EP16786753.0A patent/EP3289071A4/en not_active Withdrawn
- 2016-04-28 MX MX2017008198A patent/MX2017008198A/en unknown
- 2016-04-28 CA CA2968050A patent/CA2968050A1/en not_active Abandoned
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- 2016-04-28 AU AU2016253790A patent/AU2016253790B2/en active Active
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2019
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| CN101603020A (en) * | 2008-06-11 | 2009-12-16 | 霍夫曼-拉罗奇有限公司 | The clostridium histolyticum growth medium of no Mammals derived components |
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| FANG A等: "Production of Clostridium difficile toxin in a medium totally free of both animal and dairy proteins or digests", 《PROC NATL ACAD SCI U S A》 * |
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| TWI592486B (en) | 2017-07-21 |
| WO2016175567A1 (en) | 2016-11-03 |
| KR20160127999A (en) | 2016-11-07 |
| RU2017120815A3 (en) | 2018-12-14 |
| AU2016253790A1 (en) | 2017-05-25 |
| EP3289071A1 (en) | 2018-03-07 |
| BR112017012893A2 (en) | 2018-01-30 |
| KR101723168B1 (en) | 2017-04-05 |
| RU2679836C2 (en) | 2019-02-13 |
| TW201638330A (en) | 2016-11-01 |
| US20170260515A1 (en) | 2017-09-14 |
| US10308923B2 (en) | 2019-06-04 |
| JP2020022436A (en) | 2020-02-13 |
| AU2016253790B2 (en) | 2018-11-29 |
| CA2968050A1 (en) | 2016-11-03 |
| JP2018500881A (en) | 2018-01-18 |
| AR104418A1 (en) | 2017-07-19 |
| RU2017120815A (en) | 2018-12-14 |
| EP3289071A4 (en) | 2018-10-31 |
| MX2017008198A (en) | 2017-09-13 |
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